NM_004211.5:c.2122T>C
MANE Select
|
NP_004202.4:p.Tyr708His
|
ENST00000525748.6:c.2122T>C
MANE Select
|
ENSP00000434364.2:p.Tyr708His
|
NM_001318369.1:c.1420T>C
|
NP_001305298.1:p.Tyr474His
|
NM_001318369.2:c.1420T>C
|
NP_001305298.1:p.Tyr474His
|
NM_004211.3:c.2122T>C
|
NP_004202.2:p.Tyr708His
|
NM_004211.4:c.2122T>C
|
NP_004202.3:p.Tyr708His
|
ENST00000298923.11:c.*1419T>C
|
ENSP00000298923.7:n.*1419T>C
|
ENST00000525748.5:c.2122T>C
|
ENSP00000434364.1:p.Tyr708His
|
ENST00000528440.1:n.653T>C
|
|
XM_005253225.1:c.1420T>C
|
XP_005253282.1:p.Tyr474His
|
XM_011520473.1:c.2122T>C
|
XP_011518775.1:p.Tyr708His
|
XM_017018544.2:c.1246T>C
|
XP_016874033.1:p.Tyr416His
|
XM_017018545.2:c.1081T>C
|
XP_016874034.1:p.Tyr361His
|